Zenv is hiring Senior Officer / Executive – Regulatory Affairs for its Regulatory Affairs department.
The opportunity is open to male and female candidates with 2–4 years of relevant experience.
Candidates with a Bachelor’s or Master’s degree, including M.Pharm. and M.Sc., are eligible to apply.
Interested professionals can apply by sharing their updated resumes through the company’s recruitment email address.
Zenv Pharma Recruitment – Regulatory Affairs Department
Zenv Pharma is looking for motivated and detail-oriented professionals to join its Regulatory Affairs team. The selected candidates will be involved in regulatory submissions, licence applications, documentation, compliance activities and coordination with regulatory authorities.
| Job Details | Information |
|---|---|
| Company | Zenv Pharma |
| Department | Regulatory Affairs |
| Designation | Senior Officer / Executive |
| Experience | 2–4 Years |
| Qualification | Bachelor’s / Master’s Degree (M.Pharm. / M.Sc.) |
| Gender | Male & Female |
| Job Location | Not mentioned in the recruitment advertisement |
| Work Profile | Regulatory Affairs |
Job Role & Responsibilities
Selected candidates will handle regulatory documentation, preparation and submission of applications, follow-ups with regulatory authorities and other compliance-related activities.
Key Responsibilities
- Regulatory Application Preparation: Prepare applications for Test Licences, Additional Products, Loan Licences, Storage Licences and Certificates, and submit them through the online XLN India system.
- Licence and NOC Applications: Prepare applications such as Form CT 11, Form CT 14, Procurement NOC, Dual Use NOC and Import Licences, and submit them through the Sugam Portal.
- Regulatory Follow-ups: Coordinate and follow up with the FDA, CDSCO and NCB departments regarding submitted applications.
- Regulatory Documentation: Maintain and update records of applications submitted to local FDA, CDSCO and NCB authorities.
- DCGI Application Submissions: Prepare and submit DCGI applications for New Drugs, Subsequent New Drugs, Fixed Dose Combinations (Form CT-21) and Clinical Trial Applications (Form CT-04).
- Regulatory Query Coordination: Coordinate with applicants to address queries raised by FDA and CDSCO authorities.
- Technical Person Interviews: Plan and arrange Competent Technical Person interviews for candidates at various facilities.
- Plan Layout Approval: Arrange Plan Layout Approval meetings by coordinating with FDA and CDSCO authorities.
- Application Documentation: Prepare, review and submit hard copies of various applications.
- Additional Responsibilities: Perform other responsibilities assigned by the reporting superior.
- Regulatory Updates: Visit government websites regularly to check new regulatory circulars and guidelines.
Eligibility & Qualifications
Candidates interested in Zenv Pharma Regulatory Affairs jobs should meet the educational and experience requirements mentioned below.
Educational Qualifications
- Bachelor’s Degree
- Master’s Degree
- M.Pharm.
- M.Sc.
The recruitment advertisement does not specify particular specialisations or additional eligible disciplines.
Experience Requirements
- 2–4 years of relevant professional experience.
- Candidates should have experience or knowledge relevant to Regulatory Affairs activities.
- Understanding of regulatory submissions, licence applications and compliance documentation will be relevant to the advertised responsibilities.
Additional Requirements
- Both male and female candidates can apply.
- Candidates should be motivated and detail-oriented.
- Ability to handle regulatory documentation and application submissions.
- Coordination skills for communicating with FDA, CDSCO and NCB authorities.
- Knowledge of regulatory updates and government guidelines.
How to Apply for Zenv Pharma Recruitment
Interested and eligible candidates can submit their updated resumes directly to the company’s recruitment email address.
Email: hr@zenvisionpharma.com
Application Instructions
- Prepare your updated resume with accurate educational and professional details.
- Highlight your Regulatory Affairs experience and relevant responsibilities.
- Mention your current designation and total work experience.
- Send your updated CV to hr@zenvisionpharma.com.
Candidates are advised to ensure that their contact details and professional experience are clearly mentioned in the resume.
Frequently Asked Questions
1. Which positions are available at Zenv Pharma?
Zenv Pharma is hiring for Senior Officer / Executive positions in the Regulatory Affairs department.
2. What qualifications are required for Zenv Pharma Regulatory Affairs jobs?
Candidates with Bachelor’s or Master’s degrees, including M.Pharm. and M.Sc., can apply. Specific specialisations are not mentioned in the advertisement.
3. How much experience is required?
Candidates should have 2–4 years of experience.
4. Are freshers eligible for these vacancies?
No specific fresher eligibility is mentioned. The advertised experience requirement is 2–4 years.
5. Can male and female candidates apply?
Yes. Both male and female candidates are eligible to apply.
6. How can I apply for Zenv Pharma jobs?
Interested candidates can send their updated resumes to hr@zenvisionpharma.com.
Job Summary
| Category | Details |
|---|---|
| Company | Zenv Pharma |
| Vacancies | Senior Officer / Executive – Regulatory Affairs |
| Required Education | Bachelor’s Degree / Master’s Degree / M.Pharm. / M.Sc. |
| Experience | 2–4 Years |